MBC – the “gift” that keeps on giving

Happy September friends and family.

I feel like I missed summer so I’m being intentional about eating lunch outside in the sun! I hope you are still getting outside now and again to get some fresh air and vitamin D.

This past week was a busy one medical-wise. I had my regular monthly appointments. Additionally I had an MRI on my lumbar spine region (lower back) and met with a neuro-oncologist.

My medical oncologist is lowering the dose of one of my medications (Ibrance). There are 3 dose levels. I’ve been on this highest dose for 4 years. Apparently after being on it for that long it is common for white blood cells to start to tank (neutrophils specifically). So, I will go to the next lower dosage. It should not affect the efficacy of the treatment.

It’s interesting that the default is to start patients on the highest tolerable dose of a drug and then lower the dosage when there are side effects or complications. There is a group of patient advocates that are trying to change this so doctors don’t default to the highest dose to start.

Anyway, this change should not affect my treatment. The change will happen next month.

The neuro-oncologist believes he has found the source of my nerve pain. It appears that I have tumor on both the L3 and L4 vertebrae. The tumors are on the inside of the vertebrae and pushing on the spinal cord. That is what is generating the nerve pain in my hip and leg.

His recommendation (which I will follow) is that he do surgery to remove the tumor material. It’s not scheduled yet, hopefully will happen within 2-3 weeks.

We don’t know if the tumors are new or if they are “old” and just got pushed/moved around. The first step will be to get me out of constant pain. The second will be for my oncologist to determine if the cancer has awakened or is still sleeping. I won’t have that information until early October.

With Metastatic Breast Cancer (MBC) the cancer spreads beyond the breast. I have bone only disease. This is good in that bone only disease does not kill you. However, it can mess you up royally. The cancer in my spine has now made it very difficult to walk. The current nerve pain only allows me to lay and sleep on my left side. It’s possible though that the bone disease can cause incontinence and other very unpleasant things. So, when I say “Things could be worse.” They could, indeed.

Maddy has started her junior year of HS and a new year of dance. Evelyn is moved in to her apartment and in the thick of classes as a sophomore at University of Colorado Boulder. (She is VERY excited for the football game tomorrow! Look for her on tv.) Glen finished his fly fishing trip and will be traveling for work next week.

I have work travel scheduled (which will likely be cancelled). I also am/was planning to go to a breast cancer symposium in Pittsburgh, attending as a patient advocate. We will see how all this travel shakes out with impending surgery. I don’t have a great feeling about this travel happening either.

This back surgery is a bump in the road. One thing at a time. Thanks to everyone for your support and love. Right back at ‘ cha!

4 Comments

  1. Leysia Palen's avatar Leysia Palen says:

    Hi Donna: We love you.

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  2. ultimatesurvivorprime's avatar ultimatesurvivorprime says:

    Hi, Sweetie! Thanks so much for the informative update! I am so glad that they have found the source of the current pain. I am VERY familiar with nerve pain from that region! It’s terrible and makes it pretty impossible to do much of anything without pain. Hopefully, after this procedure, your movements will be much more comfortable, and you will be able to have a more normal activity schedule. We will be praying that is the case!

    I had bilateral injections into my SI joints this morning to determine if it will be appropriate for surgery to place implants in both sides to reduce pain and allow for more mobility. The saga continues there. The injections in my cervical C5/6 have begun to lose their positive impact on my right arm, and will likely have to be redone in another 6 weeks or so (they can only do them every 3 months). After that, if it doesn’t work for longer, I will have to have the surgery to repair those discs. Joy!

    Thanks for the updates on Maddy, Evie, Glen and the pic of Toulouse! Did you ever get a partner in crime for him?

    Wishing all the best for all of you. Much love is sent your way!

    Mom S.

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  3. seolds's avatar seolds says:

    Donna… sending love and strength for pain tolerance. I hope the surgery can be scheduled quickly to give you relief. Shell

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    1. charlevo's avatar charlevo says:

      Thank you Shelley! Looking forward to seeing you in person soon!

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